Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6)

Journal of Medical Genetics

Volumn 41, Issue 4, 2004, Pages 309-314

  Mohiddin, S A ^a   Ahmed, Z M ^b   Griffith, A J ^b   Tripodi, D ^a   Friedman, T B ^b   Fananapazir, L ^a   Morell, R J ^b  

^a NATIONAL HEART LUNG AND BLOOD INSTITUTE   (United States)

^b NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MYOSIN; MYOSIN VI; UNCLASSIFIED DRUG;

ADULT; ANAMNESIS; ARTICLE; AUDIOMETRY; AUTOSOMAL DISORDER; CHROMOSOME 6Q; CLINICAL ARTICLE; CONTROLLED STUDY; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAM; FEMALE; GENE LOCUS; GENE MUTATION; GENETIC ANALYSIS; HEART LEFT VENTRICLE HYPERTROPHY; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; MALE; MISSENSE MUTATION; PERCEPTION DEAFNESS; PHENOTYPE; PHYSICAL EXAMINATION; PRIORITY JOURNAL; QT PROLONGATION;

EID: 1942437588     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.2003.011973     Document Type: Article

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